| Meta-analysis identifies six new susceptibility loci for atrial fibrillation PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ... Nature genetics 44 (6), 670-675, 2012 | 674 | 2012 |
| Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial JD Roberts, GA Wells, MR Le May, M Labinaz, C Glover, M Froeschl, ... The Lancet 379 (9827), 1705-1711, 2012 | 462 | 2012 |
| The short QT syndrome: proposed diagnostic criteria MH Gollob, CJ Redpath, JD Roberts Journal of the American College of Cardiology 57 (7), 802-812, 2011 | 368 | 2011 |
| Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect R Tadros, C Francis, X Xu, AMC Vermeer, AR Harper, R Huurman, ... Nature genetics 53 (2), 128-134, 2021 | 171 | 2021 |
| Guidance on minimizing risk of drug-induced ventricular arrhythmia during treatment of COVID-19: a statement from the Canadian Heart Rhythm Society JL Sapp, W Alqarawi, CJ MacIntyre, R Tadros, C Steinberg, JD Roberts, ... Canadian Journal of Cardiology 36 (6), 948-951, 2020 | 134 | 2020 |
| Impact of genetic discoveries on the classification of lone atrial fibrillation JD Roberts, MH Gollob Journal of the American College of Cardiology 55 (8), 705-712, 2010 | 124 | 2010 |
| Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest C Van Der Werf, KV Lieve, JM Bos, CM Lane, I Denjoy, F Roses-Noguer, ... European heart journal 40 (35), 2953-2961, 2019 | 107 | 2019 |
| Genetic testing in the evaluation of unexplained cardiac arrest: from the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) G Mellor, ZWM Laksman, R Tadros, JD Roberts, B Gerull, CS Simpson, ... Circulation: Cardiovascular Genetics 10 (3), e001686, 2017 | 89 | 2017 |
| Association between QT-interval components and sudden cardiac death: the ARIC study (Atherosclerosis Risk in Communities) WT O˘Neal, MJ Singleton, JD Roberts, LG Tereshchenko, N Sotoodehnia, ... Circulation: Arrhythmia and Electrophysiology 10 (10), e005485, 2017 | 85 | 2017 |
| Cardiac ryanodine receptor calcium release deficiency syndrome B Sun, J Yao, M Ni, J Wei, X Zhong, W Guo, L Zhang, R Wang, D Belke, ... Science translational medicine 13 (579), eaba7287, 2021 | 73 | 2021 |
| Short-coupled ventricular fibrillation represents a distinct phenotype among latent causes of unexplained cardiac arrest: a report from the CASPER registry C Steinberg, B Davies, G Mellor, R Tadros, ZW Laksman, JD Roberts, ... European Heart Journal 42 (29), 2827-2838, 2021 | 65 | 2021 |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 65 | 2021 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 64 | 2022 |
| An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic … K Ng, EW Titus, KV Lieve, TM Roston, A Mazzanti, FH Deiter, I Denjoy, ... Circulation 142 (10), 932-947, 2020 | 56 | 2020 |
| Elevated lipoprotein (a) and risk of atrial fibrillation: an observational and Mendelian randomization study P Mohammadi-Shemirani, M Chong, S Narula, N Perrot, D Conen, ... Journal of the American College of Cardiology 79 (16), 1579-1590, 2022 | 54 | 2022 |
| Alcohol consumption and leukocyte telomere length S Dixit, MA Whooley, E Vittinghoff, JD Roberts, SR Heckbert, ... Scientific reports 9 (1), 1404, 2019 | 54 | 2019 |
| Cardiac abnormalities in first-degree relatives of unexplained cardiac arrest victims: a report from the cardiac arrest survivors with preserved ejection fraction registry C Steinberg, GJ Padfield, J Champagne, S Sanatani, P Angaran, ... Circulation: Arrhythmia and Electrophysiology 9 (9), e004274, 2016 | 54 | 2016 |
| Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy JD Roberts, JC Herkert, J Rutberg, SM Nikkel, ACP Wiesfeld, D Dooijes, ... Clinical genetics 83 (5), 452-456, 2013 | 54 | 2013 |
| Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy JD Roberts, NP Murphy, RM Hamilton, ER Lubbers, CA James, CF Kline, ... The Journal of Clinical Investigation 129 (8), 3171-3184, 2019 | 51 | 2019 |
| Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a … LA Swayne, NP Murphy, S Asuri, L Chen, X Xu, S McIntosh, C Wang, ... Circulation: Cardiovascular Genetics 10 (1), e001537, 2017 | 51 | 2017 |
